463051
Diborane
99.99% (diborane only), 9-11% (balance hydrogen), 10% in hydrogen, electronic grade
Synonym(s):
Borane (B2 H6 ), Boron hydride (B2 H6 ), Diboron hexahydride
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About This Item
Linear Formula:
B2H6
CAS Number:
Molecular Weight:
27.67
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352300
MDL number:
grade
electronic grade
assay
99.99% (diborane only)
form
gas
reaction suitability
reagent type: reductant
concentration
10% in hydrogen, 9-11% (balance hydrogen)
bp
−92.5 °C (lit.)
SMILES string
BB
InChI
1S/B2H4/c1-2/h1-2H2
InChI key
QSJRRLWJRLPVID-UHFFFAOYSA-N
General description
Atomic number of base material: 5 Boron
Application
Dibrorane gas is used primarily as a p-type dopant in the deposition of eptaxial and amorphous silicon thin films.
Useful as a p-type dopant for the deposition of silicon-containing thin films.
Packaging
Supplied in a carbon steel lecture bottle with a CGA180M/CGA110F needle valve installed.
Compatible with the following:
Compatible with the following:
- Aldrich® lecture-bottle station systems
- Aldrich® lecture-bottle gas regulators
Other Notes
See Technical Information Bulletin AL-151 Gas Regulators: Selection, Installation, and Operation
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Flam. Gas 1
Storage Class
2A - Gases
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Q Zhao et al.
Nano letters, 5(5), 847-851 (2005-05-12)
Novel carbon nanotube-metal cluster structures are proposed as prototype systems for molecular recognition at the nanoscale. Ab initio calculations show that already the bare nanotube cluster system displays some specificity because the adsorption of ammonia on a carbon nanotube-Al cluster
O H Griffith et al.
Ultramicroscopy, 6(2), 149-156 (1981-01-01)
The relative brightness of photoelectron microscopy images as a function of exposure to UV light has been determined from model systems representative of biological cell surface components. Quantitative data for amino acid homopolymers, yields. The photoelectron quantum yields, increase substantially
Holger Braunschweig et al.
Angewandte Chemie (International ed. in English), 50(52), 12613-12616 (2011-11-08)
The diboranes(4) bis(catecholato)diborane (B(2)Cat(2)) and bis(pinacolato)diborane (B(2)Pin(2)) are important precursors for organoboronic esters, which are versatile reagents for the formation of carbon-carbon bonds. A new catalytic synthesis for these compounds starts from catecholborane or pinacolborane and gives the dehydrocoupling products